Fragment-Based Design and Synthesis of Symmetrical -Peptidotriazoles Using Alkylidene -Amide Formations and Subsequent Triazole Ligation with β-Acetamido Carbonyl Scaffolds.

A novel and efficient fragment-based assembly of symmetrical -peptidotraizoles has been developed based on double Sharpless azide-alkyne click chemistry. A new Cu(II) catalyzed protocol with a wide substrate scope was developed for accessing the symmetrical alkylidene azidoamide fragment that yields the products in very good yields at room temperature without employing column purifications. The propargylated β-acetamido ketone fragment was accessed using another Cu(II) catalyzed room temperature MCR protocol.